Yoshimura Y, Ando M, Nagamatsu S, Iwashita M, Adachi T, Sueoka K, Miyazaki T, Kuji N, Tanaka M
Department of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo, Japan.
Biol Reprod. 1996 Jul;55(1):152-60. doi: 10.1095/biolreprod55.1.152.
We examined the effects of insulin-like growth factor (IGF)-I on follicular growth, oocyte maturation, and ovarian steroidogenesis and plasminogen activator (PA) activity in vitro, using a perfused rabbit ovary preparation in order to determine whether the follicle-stimulating effects of growth hormone (GH) are mediated by IGF-I. The addition of IGF-I to the perfusate stimulated follicular growth and the resumption of meiosis in follicular oocytes in a dose-dependent manner. There was no significant difference in the production of progesterone by perfused rabbit ovaries between IGF-I-treated and control ovaries, whereas IGF-I increased the production of estradiol (E2) by perfused rabbit ovaries in a dose-dependent manner. The concomitant addition of a monoclonal antibody recognizing the type I IGF receptor, alpha IR-3, to the perfusate significantly blocked IGF-I-stimulated follicular growth, oocyte maturation, and E2 production. Intrafollicular PA activity increased significantly 4 h after exposure to 10 or 100 ng/ml of IGF-I and reached maximal levels at 6 h. The percentage increase in follicle diameter at 6 h after exposure to IGF-I was significantly correlated with the intrafollicular PA activity. Treatment with GH resulted in a 2.7-fold increase in intrafollicular levels of IGF-I mRNA. The binding of [125I]-IGF-I to rabbit ovarian membrane preparations was inhibited by unlabeled IGF-I and IGF-II in a concentration-dependent manner. The relative affinity of the IGF-I receptor for IGF-I, IGF-II, and insulin was typical of type I binding (IGF-I > IGF-II > insulin). Affinity cross-linking of ovarian membranes with [125I]-IGF-I revealed a radiolabeled band corresponding to a molecular weight of 135,000, the alpha subunit of the type I IGF receptor. This band was totally displaced by IGF-I and alpha IR-3. It was concluded that IGF-I stimulated follicular development, E2 production, and oocyte maturation by interacting with its specific receptor located in rabbit ovarian membranes.
我们使用灌注兔卵巢制剂,在体外研究了胰岛素样生长因子(IGF)-I对卵泡生长、卵母细胞成熟、卵巢类固醇生成和纤溶酶原激活物(PA)活性的影响,以确定生长激素(GH)的促卵泡作用是否由IGF-I介导。向灌注液中添加IGF-I以剂量依赖的方式刺激卵泡生长和卵泡内卵母细胞减数分裂的恢复。IGF-I处理组和对照组的灌注兔卵巢孕酮生成无显著差异,而IGF-I以剂量依赖的方式增加灌注兔卵巢雌二醇(E2)的生成。向灌注液中同时添加识别I型IGF受体的单克隆抗体αIR-3,可显著阻断IGF-I刺激的卵泡生长、卵母细胞成熟和E2生成。暴露于10或100 ng/ml的IGF-I后4小时,卵泡内PA活性显著增加,并在6小时达到最高水平。暴露于IGF-I后6小时卵泡直径的增加百分比与卵泡内PA活性显著相关。用GH处理导致卵泡内IGF-I mRNA水平增加2.7倍。未标记的IGF-I和IGF-II以浓度依赖的方式抑制[125I]-IGF-I与兔卵巢膜制剂的结合。IGF-I受体对IGF-I、IGF-II和胰岛素的相对亲和力是典型的I型结合(IGF-I>IGF-II>胰岛素)。用[125I]-IGF-I对卵巢膜进行亲和交联,显示出一条对应于分子量为135,000的放射性标记带,即I型IGF受体的α亚基。这条带被IGF-I和αIR-3完全取代。得出的结论是,IGF-I通过与其位于兔卵巢膜中的特异性受体相互作用,刺激卵泡发育、E2生成和卵母细胞成熟。